Our Story
Join our team and help add tomorrows!
DAYNA'S DREAM TEAM was started in 2006 by family and friends when Dayna Jenae Blackmon was diagnosed with cystic fibrosis (CF) shortly after birth. Since that time, we have raised thousands of dollars every year in the fight to find a cure. We have been recognized in the past as Team of the Year as well as Largest Registered Team for the Poughkeepsie, New York Great Strides Walk. Dana & Jen Blackmon were great strides walk family chair's in 2012 and 2013. DAYNA'S DREAM TEAM also hosts several fund-raisers throughout the year, including our annual Benefit Monday at Mariner's Harbor event.
In 2014 DAYNA’S DREAM TEAM, has been recognized as a National Great Strides Team! We have formed new teams and will be participating in Great Strides Walk’s in Columbia, South Carolina and Gainesville, Florida!
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. We don't only walk for Dayna, we walk for them! Will you join us? All we need you to do to become a member of our team is click on the "Join our Team" button. From there you can make a donation and start your fund-raising.
By becoming a member of our team and making a donation, you are joining a growing group of people committed to finding a cure for cystic fibrosis. Together, we are adding tomorrows to the lives of people living with CF by supporting the search for a cure.
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated June 15, 2022. To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
To minimize the risk of COVID-19 infection, we ask that attendees at CF Foundation events follow these steps:
FOR YOUR SAFETY AND THE SAFETY OF OTHERS: